Ms Louise Rawcliffe BSc MBA

Programme Director

  • Louise has over 20 years’ experience in the pharmaceutical industry within regulatory affairs and regulatory compliance.

  • She has considerable knowledge of EU/US clinical trial regulations as well as medical device licensing procedures and regulations, directives and guidelines.

  • She has experience in managing compliance programmes for global clinical trials.

  • Louise has facilitated regulatory authority inspections of both UK- and US-based investigator sites and GMP and device manufacturing facilities.

  • Her extensive experience covers all phases of clinical development.

  • Louise also has 10 years’ experience in pharmacovigilance for licensed and investigational medicinal products.

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